WO2002066439A1 - Derives de pyrazole, intermediaires associes, procedes de production associes et herbicide contenant lesdits derives en tant qu'ingredient actif - Google Patents

Derives de pyrazole, intermediaires associes, procedes de production associes et herbicide contenant lesdits derives en tant qu'ingredient actif Download PDF

Info

Publication number
WO2002066439A1
WO2002066439A1 PCT/JP2002/001411 JP0201411W WO02066439A1 WO 2002066439 A1 WO2002066439 A1 WO 2002066439A1 JP 0201411 W JP0201411 W JP 0201411W WO 02066439 A1 WO02066439 A1 WO 02066439A1
Authority
WO
WIPO (PCT)
Prior art keywords
group
carbon atoms
substituted
yield
general formula
Prior art date
Application number
PCT/JP2002/001411
Other languages
English (en)
Japanese (ja)
Inventor
Kenji Hirai
Atsushi Uchida
Atsuko Watanabe
Taeko Abe
Takuya Ueda
Hiroshi Ito
Original Assignee
Sagami Chemical Research Center
Kaken Pharmaceutical Co., Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sagami Chemical Research Center, Kaken Pharmaceutical Co., Ltd. filed Critical Sagami Chemical Research Center
Priority to US10/468,527 priority Critical patent/US7700786B2/en
Priority to AT02712451T priority patent/ATE504573T1/de
Priority to DE60239667T priority patent/DE60239667D1/de
Priority to JP2002565956A priority patent/JP4249982B2/ja
Priority to BR0207412-5A priority patent/BR0207412A/pt
Priority to EP02712451A priority patent/EP1362852B1/fr
Publication of WO2002066439A1 publication Critical patent/WO2002066439A1/fr
Priority to US12/713,421 priority patent/US20100152443A1/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/18—One oxygen or sulfur atom
    • C07D231/20—One oxygen atom attached in position 3 or 5

Definitions

  • the present invention relates to pyrazole derivatives, intermediates for producing the same, methods for producing them, and herbicides containing them as active ingredients.
  • the present invention relates to novel pyrazole derivatives, intermediates for producing the same, methods for producing them, and herbicides containing them as active ingredients.
  • pyrazole derivatives having physiological activity as a pesticide such as herbicidal activity and insecticidal activity have been known.
  • a pyrazole derivative at the 3-position of the pyrazole ring There are no reports on substituted oxy groups and pyrazole derivatives having a substitution force rubamoyl group or substituted thiocarbamoyl group on the 1-position nitrogen atom, and no reports on their biological activities.
  • Examples of the pyrazole derivative having a structure similar to the pyrazole derivative (1) of the present invention include those described in WO97 / 24332 (EP 876351, JP 2000/502686, US 6075149) and EP 256667 (JP 63/044571, US 5374644). Although pyrazole derivatives are known, they are completely different from the pyrazole derivative (1) of the present invention in having an alkyl group on the nitrogen atom of the pyrazole ring. Furthermore, although the pyrazole derivatives described in the above-mentioned WO 97/24332 and EP 256667 are described as having fungicidal and activity against pests, there is no description concerning other biological activities. Disclosure of the invention
  • the present invention provides a novel pyrazole derivative having excellent herbicidal activity and high crop selectivity, an intermediate for producing the same, a process for producing the same, and a herbicide containing these derivatives as an active ingredient.
  • the present inventors have conducted intensive studies for herbicides having excellent herbicidal activity and crop selectivity.
  • the pyrazol derivative of the present invention represented by the following general formula (1) causes crop damage.
  • the present invention has been found to show excellent herbicidal activity without application at a low dose, and to find a simple production method for these.
  • the present invention provides a compound represented by the general formula (1):
  • R 1 is a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, an optionally substituted cycloalkyl group having 3 to 8 carbon atoms, an alkyloxy having 1 to 6 carbon atoms.
  • R 2 represents a hydrogen atom, a halogen atom, or an optionally substituted alkyl group having 1 to 6 carbon atoms
  • R 3 represents a hydrogen atom
  • An alkyl group having 1 to 12 carbon atoms which may be substituted a cycloalkyl group having 3 to 8 carbon atoms which may be substituted, an aralkyl group having 7 to 11 carbon atoms which may be substituted
  • R 1 R 2 and R 5 represent the same meaning as described above.
  • R 5 has the same meaning as described above; Z represents a leaving group.
  • R 1 represents the same meaning as described above;
  • R 5a represents a hydrogen atom, an optionally substituted phenyl group, or an optionally substituted pyridyl group.
  • R 1 and R 5 a have the same meanings as defined above.
  • R 2 a represents a halogen atom.
  • R 3a -NCY (5) (wherein, R 3 a is optionally substituted alkyl group having 1 to 12 carbon atoms, optionally substituted cycloalkyl group having a carbon number of 3-8, optionally substituted Aralkyl group having 7 to 11 carbon atoms, alkenyl group having 3 to 6 carbon atoms which may be substituted, alkynyl group having 3 to 6 carbon atoms which may be substituted, phenyl which may be substituted Group, an optionally substituted alkyloxy group having 1 to 6 carbon atoms, an optionally substituted cycloalkyloxy group having 3 to 8 carbon atoms, an optionally substituted aralkyloxy group having 7 to 11 carbon atoms Group, an optionally substituted alkenyloxy group having 3 to 6 carbon atoms, an optionally substituted carbon Represents an alkynyloxy group of the number 3 to 6 or a phenyloxy group which may be substituted; Y represents the same meaning as described above.
  • R 1 R 2, R 3 a, R 5 a and Y represent. As defined above, relates to a process for preparing pins Razoru derivative represented by the.
  • R 1, R 2, R 3 a and R 5 represents. As defined above, relates to a process for preparing pyrazole Lumpur derivative represented by.
  • R 4 a is alkyl group which carbon atoms 1 to 1 be 2-substituted, cycloalkyl group substituted carbon atoms and optionally 3-8, carbon atoms and may be substituted 7-1 1 represents an aralkyl group, an optionally substituted alkenyl group having 3 to 6 carbon atoms or an alkynyl group having 3 to 6 carbon atoms which may be substituted, and Z represents a leaving group. Is reacted in the presence of a base to obtain a compound represented by the general formula (lc) of the present invention.
  • R 1 R 2 , R 3a , R 4a , R 5 and Y represent the same meaning as described above).
  • R 3 b and R 4 b is an optionally substituted alkyl group having 1 to 12 carbon atoms, optionally substituted good carbon number 3-8 cycloalkyl group, an optionally substituted carbon
  • An aralkyl group having 1 to 11 carbon atoms, an alkenyl group having 3 to 6 carbon atoms which may be substituted, an alkynyl group having 3 to 6 carbon atoms which may be substituted, or a phenyl group which may be substituted represents.
  • R 3 b and R 4 b is reacted force Luba Min acid chlorides represented by the heterocycles may be formed.
  • the present invention provides a compound represented by the general formula (2d), which is an intermediate for producing the pyrazole-1-carboxamide derivative of the present invention.
  • RR 2 and R 5 have the same meanings as described above.
  • R 3 e is a hydrogen atom, an optionally substituted alkyl group having 1 to 12 carbon atoms, an optionally substituted cycloalkyl group having 3 to 8 carbon atoms, an optionally substituted carbon number
  • R 3 R 4 R 5 and Y are as defined above.
  • R 2 b represents. A halogen atom) a method for producing a pyrazole derivative represented by the.
  • the present invention relates to a method for producing a pyrazole-1-carboxamide derivative represented by the formula:
  • the present invention relates to a herbicide containing a pyrazole derivative as an active ingredient.
  • the alkyl group having 1 to 6 carbon atoms represented by R 1 , R 2 and R 2a may be linear or branched, and may be a methyl group, an ethyl group, a propyl group or an isopropyl group.
  • alkyl groups may be substituted with a halogen atom, an alkyloxy group having 1 to 6 carbon atoms, a formyl group, an alkyloxycarbonyl group having 1 to 6 carbon atoms, a heterocyclic ring, or the like. Include trichloromethyl, trifluoromethyl, methoxymethyl, ethoxymethyl, 2-methoxyethyl, formylmethyl, methoxycarbonylmethyl, ethoxycarbonylmethyl, furfuryl, tetrahydrofurfuryl, and 2-picolyl. Groups, 3-picolyl group, 4-picolyl group, 2-phenylmethyl group, 2-morpholinoethyl group and the like.
  • R 3, R 3 a, R 3 b, as R 3 C, R 4, R 4 alkyl Le group having 1 to 12 carbon atoms represented by a and R 4 b are each linear or branched Methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, tributyl, pentyl, isoamyl, neopentyl, 1-ethylpropyl, 1 -Methylbutyl group, 2-methylbutyl group, hexyl group, isohexyl group, 2-ethylbutyl group, 4-methylpentyl group, heptyl group, trimethylhexyl group, octyl group, decyl group, pendecyl group, dodecyl group Etc.
  • alkyl groups include a halogen atom, a cycloalkyl group having 3 to 8 carbon atoms, a cyano group, a nitro group, an alkylthio group having 1 to 6 carbon atoms, an alkyloxy group having 1 to 6 carbon atoms, and an alkyloxy group having 1 to 6 carbon atoms.
  • One or more of these may be substituted with a cyclical group, a carboxy group, an acyl group, or the like, and more specifically, a 2-chloroethyl group, a 2-bromoethyl group, a 3-chloropropyl group, a 3-fluoropropyl group, or a cyclopropyl group.
  • Examples thereof include a cyclopropyl group, a 2-methoxycarbonylcyclopropyl group, a 2-cyanocyclopropyl group, a 2-methylcyclopentyl group, and a 3-methylcyclopentyl group.
  • a halogen atom, an alkyl group having 1 to 12 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, an alkyloxy group having 1 to 6 carbon atoms, a haloalkyloxy group having 1 to 6 carbon atoms are present on the aromatic ring of these aralkyl groups.
  • c may be substituted one or more, such as a benzyl group, a 2-fluorobenzyl group, a 3-fluorobenzyl group, a 4_fluorobenzyl group, a 2-chlorobenzyl group, 3-chlorobenzyl, 4-bromobenzyl, 2-bromobenzyl, 3-bromobenzyl, 4-bromobenzyl, 3,5-difluorobenzyl, 3,5-dichlorobenzyl Benzyl group, 3,5-dibromobenzyl , 2-methylbenzyl, 3-methylbenzyl, 4-methylbenzyl, 2,4-dimethyl
  • Examples of the alkenyl group having 3 to 6 carbon atoms represented by R 3 include an aryl group, a 2-methyl-2-propenyl group, a 2-butenyl group, a 3-butenyl group, a 2-pentenyl group, and a 3-pentenyl group. Group, 2-hexenyl group, 3-hexenyl group and the like. These alkenyl groups may be substituted with a halogen atom or the like, for example, 2-chloro-2-propenyl group, 3-chloropropenyl group, 4-chloro-2-butenyl group. And the like.
  • alkenyl groups may be substituted with a halogen atom or the like, for example, 2-chloro-2-propenyl group, 3-chloropropenyl group, 4-chloro-2-butenyl group.
  • R 3 which like can be exemplified, 3 ⁇ R 3 b, as the R 3 c, R 4, R 4 alkynyl group having 3 to 6 carbon atoms represented by a and R 4 b, linear Or a branched one, such as propargyl, 1-butyn-3-yl, 3-methyl-1-butyn-3-yl, 2-butynyl, and 2-pentynyl And a 3-pentenyl group.
  • alkynyl groups may be substituted with a halogen atom or the like, for example, a 3-fluoro-2-propynyl group, a 3-chloro-2-propynyl group, a 3-bromo_2-propynyl group, Examples thereof include a 4-bromo-2-butynyl group and a 4-bromo-3-butynyl group.
  • R ⁇ R 3, R 3 a , R 3 b may off be substituted represented by z R 4 and R 4 b
  • the phenyl group include a halogen atom, an alkyl group having 1 to 12 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, an acyl group having 1 to 6 carbon atoms, and a C1-C12 alkyl group substituted with alkyloxy imino group, C1-C6 alkyloxy carbonyl group, carboxy group, cyano group, C1-C6 alkyloxy group, aryloxy Group, haloalkyloxy group having 1 to 6 carbon atoms, alkylthio group having 1 to 6 carbon atoms, alkylsulfinyl group having 1 to 6 carbon atoms, alkylsulfonyl group having 1 to 6 carbon atoms, halo having 1 to 6 carbon atoms Examples thereof include an alkylthio group, a hal
  • a phenyl group which may be substituted represented by R 5 and R 5 a, as a substituent on benzene ring, a halogen atom, the number 1 to 1 2 alkyl group having a carbon haloalkyl carbon number 1-6 Group, C1-C6 acyl group, C1-C4 alkyloxyimino group substituted C1-C12 alkyl group, C1-C6 alkyloxycarbonyl group A carboxy group, a cyano group, a substituted amino group, an alkyloxy group having 1 to 6 carbon atoms, an aryloxy group, a haloalkyloxy group having 1 to 6 carbon atoms, an alkylthio group having 1 to 6 carbon atoms, and an alkylthio group having 1 to 6 carbon atoms.
  • alkylsulfinyl group an alkylsulfonyl group having 1 to 6 carbon atoms, a haloalkylthio group having 1 to 6 carbon atoms, a haloalkylsulfinyl group having 1 to 6 carbon atoms, a haloalkylsulfonyl group having 1 to 6 carbon atoms, a nitro group, etc. Fenuru having It can be exemplified. Substituents on these benzene rings Electron-withdrawing groups such as trifluoromethyl group, nitro group, cyano group, chlorine atom, fluorine atom and alkyloxycarbonyl group have good reaction yield and easy access to raw materials.
  • substitution positions of these electron-withdrawing groups are preferably at the ortho position and the Z or para position. More specifically, 4-fluorophenyl group, 4-chlorophenyl group, 4-bromophenyl group, 2,4-difluorophenyl group, 2,4-dichlorophenyl group, 2,4,5-trichlorophenyl group Group, 2-chloro-5-trifluoromethylphenyl group, 2-trifluoromethylphenyl group, 4-trifluoromethylphenyl group, 2,4-bis (trifluoromethyl) phenyl group, 2, 6- Dichloro mouth 4-trifluoromethylphenyl, 4-cyanophenyl, 4-cyano-2-trifluoromethylphenyl, 2-methylthiophenyl, 4-methylthiophenyl, 2-methylthiophene 2-phenyl, 4-methylsulfinylphenyl, 2-methylsulfonylphenyl, 4-methylsulfonylphenyl, 4-trifluor
  • the substituents on these benzene rings can be converted to amino groups by reducing the nitro group, for example, and the amino groups can be converted to halogen atoms or substituted alkyl groups via diazonium salts. These can also be exemplified as substituents on the benzene ring.
  • the optionally substituted pyridyl group represented by R 5 and R 5 a as a substituent on pyridinium 'ring, a halogen atom, an alkyl group having 1 to 12 carbon atoms, a haloalkyl group having carbon . ⁇ 6, 1 to 6 carbon atoms, 1 to 4 carbon atoms
  • Substituents on these pyridine rings include electron-withdrawing groups such as trifluoromethyl, nitro, cyano, chlorine, fluorine, and alkyloxycarbonyl groups, which provide good reaction yields and easy availability of raw materials. And the substitution position of these electron-withdrawing groups is preferably the 3-position and Z- or 5-position of the pyridine ring.
  • 3-chloropyridine-2-yl group 5-chloropyridine-2-yl group, 3,5-dichloropyridin-2-yl group, 4-amino-3,5 -Dichloropyridine-2-yl group, 3-cyano-6-methylpyridine-2-yl group, 5-trifluoromethylpyridine-2-yl group, 3-chloro-5-trifluoromethylpyridine + 2-yl, 3-nitro-2-yl, 5-nitropyridine-2-yl, 3-nitro-4-methylpyridine-2-yl, 3-nitro-6-methoxypyridine- 2-yl, 2-chloro-3-nitropyridin-6-yl, 6-chloro-3-nitropyridin-2-yl, 3,5-dinitropyridine-2-yl And the like.
  • substituents on these pyridine rings for example, nitro groups can be converted to amino groups by reduction, and amino groups can be converted to halogen atoms or substituted alkyl groups via diazonium salts. These can also be exemplified as substituents on the pyridine ring.
  • the alkyl group forming these alkyloxy groups include a halogen atom, a cycloalkyl group having 3 to 8 carbon atoms, an alkyloxy group having 1 to 6 carbon atoms, C1-C6 alkylthio group, C1-C6 alkyloxycarbonyl group, carboxy group, cyano group, nitro group, amino group which may be substituted, phenyl group which may be substituted, etc. May be substituted one or more
  • R 3 is a cycloalkyl O alkoxy group R 3 a and R 3 carbon atoms represented by e. 3 to 8, cyclopropyl O alkoxy group, cyclobutyl O alkoxy group, a cyclopentyl Okishi group, Kishiruokishi group cyclohexylene, A cyclooctyloxy group and the like can be exemplified. Further, these cycloalkyl groups may be substituted with a halogen atom, an alkyl group having 1 to 4 carbon atoms, an alkyloxycarbonyl group having 1 to 4 carbon atoms, a cyano group, and the like.
  • 1,1-methylcyclopropyl pyroxy 2,2-dimethylcyclopropyloxy, 2-chlorocyclopropyloxy, 2,2-dichlorocyclopropyloxy, 2-methoxycarboylcyclopropyloxy, 2-sia
  • Examples thereof include a nocyclopropyloxy group, a 2-methylcyclopentyloxy group, and a 3-methylcyclopentyloxy group.
  • R 3 e The R 3, R 3 a and Ararukiruokishi group having a carbon number of 7 to 1, represented by R 3 e, Benjiruokishi group, 1-phenylpropyl E chill O alkoxy group, 2 - phenylalanine E chill O alkoxy group, 1 -Phenylpropyloxy, 1-naphthylmethyloxy, 2-naphthylmethyloxy and the like.
  • a halogen atom, an alkyl group having 1 to 12 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, an alkyloxy group having 1 to 6 carbon atoms, and a haloalkyloxy group having 1 to 6 carbon atoms are present on the aromatic ring of these aralkyloxy groups.
  • R 3 a is Arukeniruokishi group having 3 to 12 carbon atoms represented by a and R 3 e, it may be straight chain or branched or cyclic, Bok pro base two Ruokishi group , Aryloxy, 2-methyl-2-propenyloxy, 2-butenyloxy, 3-butenyloxy, 2-pentenyloxy, 3-pentenyloxy, 1-cyclopentenyloxy, and 2- Examples thereof include a xenyloxy group, a 3-hexenyloxy group, a tricyclohexenyloxy group, a 2-heptenyloxy group, and a tricyclooctenyloxy group.
  • alkenyl groups may be substituted with a halogen atom or the like, for example, 2-chloro-2-propenyloxy group, 3-chloropropenyloxy group, 4-chloro-2-butenyloxy group. And the like.
  • the alkynyloxy group having 3 to 6 carbon atoms represented by R 3 , R 3a and R 3e may be linear or branched, and may be a propargyloxy group,
  • Examples thereof include a 1-butyn-3-yloxy group, a 3-methyl-1-butyn-3-yloxy group, a 2-butynyloxy group, a 2-pentynyloxy group, and a 3-pentynyloxy group.
  • These alkynyl groups may be substituted with a halogen atom or the like, for example, 3-fluoro-2-propynyloxy group, 3-chloro-
  • Examples thereof include a 2-propynyloxy group, a 3-bromo-2-propieroxy group, a 4_bromo_2-butynyloxy group, and a 4-bromo-3-butinyloxy group.
  • the R 3 and R 4, R 3 heterocyclic ring e and R 4 and R 3 b and R 4 b is formed together with the nitrogen atom to which are attached, pyrrole, pyrroline, pyrrolidine, imidazole, imidazoline, Imidazolidines, pyrazoles, pyrazolines, pyrazolidines, piperidines, piperazines, indole, indolines, isoindoles, 1H-indazols, purines, oxazolines, isoxazolines, isooxazolidines, thiazolines, morpholines, thiomorpholines, aziridines, aziridines , Tetrahydrooxazine, etc., which are an alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, a halogen atom, One or more may be substituted with a cyano group or the like.
  • the halogen atom represented by R 2 and R 2 b can be exemplified a chlorine atom, a bromine atom, a full Tsu atom and the like.
  • Examples of the leaving group represented by Z include a halogen atom such as a chlorine atom, a bromine atom and an iodine atom, or a methylsulfonyloxy group, a trifluoromethylsulfonyloxy group, a phenylsulfonyloxy group, and a p-tolylsulfonyl.
  • Examples thereof include an alkyl group such as an alkoxy group and an arylsulfonyloxy group.
  • Step-1 shows a method for producing a pyrazole derivative (2) of the present invention by reacting a pyrazole derivative (3) with a compound (4) in the presence of a base.
  • This reaction must be carried out in the presence of a base.
  • a base examples include sodium hydride, sodium amide, sodium carbonate, potassium carbonate, sodium methoxide, sodium ethoxide, potassium-1-butoxide, sodium hydroxide, and water.
  • Alkali metal bases such as potassium oxide, and organic amines such as triethylamine, triptylamine, N-methylmorpholine, pyridine, and dimethylaniline can be used. It is preferable to use a base in an amount equal to or more than the amount of the reaction substrate in terms of good yield.
  • the reaction is preferably performed in a solvent, and any solvent that does not harm the reaction can be used.
  • a solvent for example, getyl ether, tetrahydrofuran (THF), dioxane, ether solvents such as 1,2-dimethoxyethane (DME), nitriles such as acetonitrile and propionitrile, esters such as ethyl acetate and ethyl propionate, benzene, toluene,
  • Use aromatic hydrocarbon solvents such as xylene and black benzene, amides such as N, N-dimethylformamide (DMF) and N-methylpyrrolidone, dimethyl sulfoxide (DMS0), water, or a mixture of these.
  • the reaction temperature is not particularly limited, but the reaction can be carried out at a temperature appropriately selected from the range of 0 ° C to 150 ° C to obtain the desired product in good yield.
  • the desired product can be obtained by a usual post-treatment operation.
  • the target product can be purified by column chromatography or recrystallization.
  • the pyrazolyl derivative represented by the general formula (3) as a raw material in this step is, for example, a ring of hydrazine and a / 3-ketoester derivative described in Organic Synthes is, Vol. 6, 791 (1988). It can be easily produced by a chemical reaction.
  • the obtained 3-hydroxypyrazol derivative (3) exists as an equilibrium mixture with a normal tautomer, but is represented by the structure of the alcohol (3) in the general formula for convenience.
  • Production method 2 (step-2) shows a method for producing the pyrazole derivative (2b) of the present invention by halogenating the pyrazole derivative (2a).
  • R 1, R 2 a and R 5 a have the same meanings as defined above.
  • Halogenation can be carried out using a halogenating agent.
  • a halogenating agent sulfuryl chloride, N-chlorosuccinimide, N-bromosuccinimide and the like can be used.
  • the reaction is preferably performed in a solvent, and any solvent that does not harm the reaction can be used.
  • a solvent such as pentane, hexane, and octane
  • Aromatic hydrocarbon solvents such as dimethyl ether, tetrahydrofuran, dioxane, DME, etc.
  • halogen solvents such as dichloromethane, chloroform, carbon tetrachloride, etc.
  • aromatic hydrocarbons such as chlorobenzene, dichlorobenzene, etc.
  • examples thereof include a solvent, an organic acid-based solvent such as acetic acid and propionic acid, water, and a mixed solvent thereof.
  • step-3 is a step of producing the pyrazole derivative (la) of the present invention by reacting the pyrazole derivative (2c) with an isocyanate or an isothiocyanate (5). .
  • R 1, R 2, R 3 a, R 5 a and Y are as defined above.
  • This reaction can be carried out in the presence of a base.
  • a base examples include sodium hydride, sodium amide, sodium carbonate, potassium carbonate, sodium methoxide, sodium ethoxide, potassium-1-butoxide, and sodium hydroxide.
  • alkali metal bases such as potassium hydroxide and the like, and organic amines such as triethylamine, triptylamine, N-methylmorpholine, pyridine and dimethylaniline.
  • the amount of the base used is not particularly limited.
  • the reaction can be performed in a solvent, and any solvent that does not harm the reaction can be used.
  • the solvent include ether solvents such as dimethyl ether, THF, dioxane, DME, etc., acetonitrile, propionitol Nitriles such as ethyl, esters such as ethyl acetate and ethyl propionate, aromatic hydrocarbon solvents such as benzene, toluene, xylene, and benzene, halogens such as dichloromethane, chloroform, and carbon tetrachloride Solvents, DMF, amides such as N-methylpyrrolidone, DMS0, or a mixed solvent thereof can be used.
  • the reaction temperature is not particularly limited, but the reaction can be carried out at a temperature appropriately selected from the range of 0 ° C to 150 ° C to obtain the desired product in good yield.
  • the desired product can be obtained by a usual post-treatment operation, but if necessary, it can be purified by column chromatography or recrystallization.
  • Production method 14 shows a method for producing the pyrazole derivative (lb) of the present invention by reacting the pyrazole derivative (3a) with the compound (4) in the presence of a base.
  • This reaction must be carried out in the presence of a base.
  • a base examples include sodium hydride, sodium amide, sodium carbonate, potassium carbonate, sodium methoxide, sodium ethoxide, potassium-1-butoxide, sodium hydroxide, and water.
  • Alkali metal bases such as potassium oxide, and organic amines such as triethylamine, triptylamine, N-methylmorpholine, pyridine, and dimethylaniline can be used. It is preferable to use a base in an amount equal to or more than the amount of the reaction substrate in terms of good yield.
  • the reaction is preferably performed in a solvent, and any solvent that does not harm the reaction can be used.
  • a solvent for example, dimethyl ether, tetrahydrofuran (THF), dioxane, 1,2-dimethoxyethane (DME), etc.
  • Ether solvent of the Nitriles such as cetonitrile and propionitrile, esters such as ethyl acetate and ethyl propionate, aromatic hydrocarbon solvents such as benzene, toluene, xylene, and chlorobenzene, N, N-dimethylformamide (DMF ), Amides such as N-methylpyrrolidone, dimethylsulfoxide (DMS0), water, or a mixed solvent thereof.
  • the reaction temperature is not particularly limited, but the reaction can be carried out at a temperature appropriately selected from the range of 0 ° C to 150 ° C to obtain the desired product in good yield.
  • the desired product can be obtained by a usual post-treatment operation, but if necessary, it can be purified by column chromatography or recrystallization.
  • Production method-5 shows a method for producing a pyrazole derivative (lc) of the present invention by reacting a pyrazole derivative (lb) with a compound (6) in the presence of a base.
  • R 1 , R 2 , R 3a , R 4a , R 5 , Y and Z have the same meanings as described above.
  • a base Sodium hydride, sodium amide, sodium carbonate, potassium carbonate, sodium methoxide, sodium ethoxide, alkali metal bases such as potassium-1-butoxide, sodium hydroxide, potassium hydroxide, etc., triethylamine, triptylamine, N-methylmorpholine Organic amines such as pyridine, dimethylaniline and the like can be used.
  • the target compound can be obtained in good yield by carrying out the reaction using a base in an equivalent amount or more with respect to the reaction substrate.
  • the reaction is preferably performed in a solvent, and any solvent that does not harm the reaction can be used.
  • solvent such as getyl ether, THF, DME, and dioxane; acetonitrile, propionitrile, and the like.
  • Nitrile Aromatic hydrocarbon solvents such as benzene, toluene, xylene, and benzene, amides such as DMF and N-methylpyrrolidone, DMS0, water, and a mixed solvent thereof.
  • the reaction temperature is not particularly limited, but by reacting at a temperature appropriately selected from the range of 0 ° C to 100 ° C, the desired product can be obtained in high yield. After completion of the reaction, the desired product can be obtained by a usual post-treatment operation, but if necessary, it can be purified by column chromatography or recrystallization.
  • the production method-6 shows a method for producing the pyrazole derivative (Id) of the present invention by reacting the pyrazolyl derivative (2) with the rubbamate chlorides (7) in the presence of a base. .
  • R 2 , R 3b , R 4b and R 5 represent the same meaning as described above.
  • This reaction must be carried out in the presence of a base.
  • the base include sodium hydride, sodium amide, sodium carbonate, potassium carbonate, sodium methoxide, sodium ethoxide, potassium-1-butoxide, sodium hydroxide, and water.
  • Alkali metal bases such as potassium oxide, and organic amines such as triethylamine, triptylamine, N-methylmorpholine, pyridine, and dimethylaniline can be used.
  • the target compound can be obtained in good yield by carrying out the reaction using a base in an equivalent amount or more with respect to the reaction substrate.
  • the reaction is preferably performed in a solvent, and any solvent that does not harm the reaction can be used.
  • solvents such as getyl ether, THF, DME, and dioxane; acetonitrile, propionitrile, and the like.
  • the reaction temperature is not particularly limited, but the desired product can be obtained in good yield by reacting at a temperature appropriately selected from the range of 0 ° C to 100 ° C. After completion of the reaction, the desired product can be obtained by a usual post-treatment operation, but if necessary, it can be purified by column chromatography or recrystallization.
  • the pyrazole derivative (2) is reacted with phosgene or a phosgene equivalent such as phosgene dimer or phosgene trimer to produce the pyrazole derivative (2d) of the present invention which is a production intermediate ( Step 17)
  • phosgene or a phosgene equivalent such as phosgene dimer or phosgene trimer
  • R 1 , R 2 , R 3 R 4 and R 5 represent the same meaning as described above.
  • Step 17 In the reaction of step 7, halogen-based solvents such as dichloromethane, chloroform, carbon tetrachloride, etc., aromatic hydrocarbon solvents such as benzene, toluene, xylene, and cyclobenzene, or ester-based solvents such as ethyl acetate and propyl acetate
  • the target compound can be synthesized by reacting the pyrazole derivative (2) with phosgene or a phosgene equivalent in a solvent.
  • the reaction temperature is not particularly limited, but the desired product can be obtained in good yield by reacting at a temperature appropriately selected from the range of -30 ° C to 150T. After completion of the reaction, the desired product can be obtained by a usual post-treatment operation, but the product can be used as it is in the next reaction without isolation.
  • Step-8 It is essential that the reaction of Step-8 be carried out in the presence of a base.
  • the base include sodium hydride, sodium amide, sodium carbonate, potassium carbonate, potassium-tobutoxide, sodium hydroxide, potassium hydroxide and the like.
  • Organic amines such as alkali metal bases, triethylamine, triptylamine, N-methylmorpholine, pyridine and dimethylaniline can be used.
  • the target compound can be obtained in good yield by carrying out the reaction using an equivalent amount or more of the base to the reaction substrate.
  • the reaction is preferably performed in an organic solvent, such as benzene, toluene, xylene, THF, getyl ether, chloroform, dichloromethane, methanol, ethanol, propyl alcohol, isopropyl alcohol, t-butyl alcohol, ethyl acetate, DMF DMS0 or the like can be used.
  • organic solvent such as benzene, toluene, xylene, THF, getyl ether, chloroform, dichloromethane, methanol, ethanol, propyl alcohol, isopropyl alcohol, t-butyl alcohol, ethyl acetate, DMF DMS0 or the like can be used.
  • the reaction can be carried out at a temperature appropriately selected from the range of room temperature to the reflux temperature of the solvent.
  • the desired product can be obtained by a usual post-treatment operation, but if necessary, it can be purified by column chromatography or recrystallization.
  • Production method_8 shows a method for halogenating the pyrazole derivative (If) to produce the pyrazole derivative (lg) of the present invention.
  • Halogenation can be carried out using a halogenating agent.
  • a halogenating agent sulfuryl chloride, N-chlorosuccinimide, N-bromosuccinimide and the like can be used.
  • the reaction is preferably performed in a solvent, and any solvent that does not harm the reaction can be used.
  • solvents include aliphatic hydrocarbon solvents such as pentane, hexane, and octane, getyl ether, tetrahydrofuran, and dioxane. , DME, etc., ether solvents, dichloromethane, chloroform, carbon tetrachloride, etc., halogenated solvents, chlorobenzene, dichlorobenzene, etc., aromatic hydrocarbons
  • reaction temperature varies depending on the halogenating agent used, and is selected from the range of -10 ° C to 150 ° C. It is preferable because the rate is good.
  • the desired product can be obtained by a usual post-treatment operation, but if necessary, it can be purified by column chromatography or recrystallization.
  • Production method 19 shows a method for producing the pyrazole derivative (li) of the present invention by oxidizing the thiocarbonyl group of the pyrazole derivative (lh).
  • the oxidation of the thiocarbonyl group can be performed using an oxidizing agent.
  • an oxidizing agent for example, aqueous hydrogen peroxide can be used.
  • the reaction is preferably carried out in a suitably selected ratio of aqueous alcohol, and methanol, ethanol, propanol or the like can be used.
  • This reaction is preferably carried out in the presence of a base.
  • a base sodium hydroxide, potassium hydroxide or the like can be used.
  • the reaction can be carried out at a temperature appropriately selected from the range of -30 ° C to 60.
  • the desired product can be obtained by a usual post-treatment operation, but if necessary, it can be purified by column chromatography or recrystallization.
  • Example 1-5 4_fluoro-3-nitrobenzotrifluoride and a 3-hydroxypyrazole derivative (Example 1-6: 3-hydroxy-5-trifluoromethylpyrazole, Example 7: 5-ethyl) 3-hydroxypyrazole, Example 8: 4,5-dimethyl-3-hydroxypyrazole, Example 1 9: 4-Ethyl-3_hydroxy-5-methylpyrazole) to give the corresponding 3- An aryloxypyrazole derivative was obtained.
  • the product / shape / yield / melting point / NMR spectrum is described below.
  • Example 11 2-Fluoro-5-nitrobenzotrifluoride and a 3-hydroxypyrazole derivative (Example 11: 5-ethyl-3-hydroxypyrazol, Example 11) : 4,5-dimethyl-3-hydroxypyrazole, Example 1 ° 3 ⁇ 4 ffi named ⁇ (sx woo ⁇ e digging, 3 ⁇ 4) (TOOZ) mm-m ⁇ ⁇ -m ⁇
  • Chrysanthemum gi. 3 ⁇ 4 ⁇ ⁇ 1 ⁇ ⁇ 3 ⁇ 4 (101111110 '1 9' ⁇ 6 ⁇ ⁇ 6) ⁇ ⁇ ⁇ ⁇ -' ⁇ ⁇ (I 0 orchid S' ⁇ ' ⁇ 9 ⁇ ⁇ )) ⁇ ⁇ fM -'i 9 ⁇ thigh ( ⁇ ) jiang 0) (louiino ' ⁇ 9' ⁇ 009) ⁇ (--9- ⁇ ⁇ mouth:
  • Example 19 5-ethyl-3-hydroxypyrazole, Example 1 20: 3-hydroxy-5_
  • Example 19 5-ethyl-3-hydroxypyrazole, Example 1 20: 3-hydroxy-5_
  • Example 19 5-ethyl-3-hydroxypyrazole
  • Example 1 20 3-hydroxy-5_
  • Example 19 5-ethyl-3-hydroxypyrazole
  • Example 1 20 3-hydroxy-5_
  • Example 19 5-ethyl-3-hydroxypyrazole
  • Example 1 20 3-hydroxy-5_
  • Example 19 4-Ethyl-3-hydroxy-5-methylvirazole
  • Example—24 3-Hydroxy5- (methoxymethyl) pyrazole
  • Example 1 25 ( 3-Hydroxypyrazol-5-yl) ethyl acetate
  • Example 1 26 3-Methyl hydroxypyrazol-5-carboxylate
  • Example 1 27 4,5-dimethyl-3-hydroxy Pyrazole
  • Example 1 28 4-Ethyl-3-hydroxy-5-methylvirazole
  • Example 1 29 reacting with 5-
  • Example 1 In the same manner as in Example 33, 3-hydroxy-5-methylvirazole and a pyridine derivative (Example 34: 2-chloro-6-methoxy-3-nitropyridine; Example 35: 2-chloropyridine) -4_methyl-5-nitropyridine) to give the corresponding 3-aryloxypyrazole derivatives, respectively.
  • the product / shape / yield / melting point / NMR spectrum is described below.
  • Example 35 2,3-dichloro-5-trifluoromethylpyridine and a 3-hydroxypyrazole derivative
  • Example 36 3-hydroxy-5-trifluoromethylpyrazole
  • Example 1 37 5- Respectively, by reacting ethyl-3-hydroxypyrazole,
  • Example 1 38 4,5-dimethylpyrazole-3-hydroxy
  • Example 39 4-ethyl-3-hydroxy-5-methylpyrazole.
  • the corresponding 3-aryloxypyrazole derivative was obtained.
  • generate The product / shape / yield / melting point / NMR spectrum is described.
  • Example 1 In the same manner as in Example 40, 3- (5-fluoro-2-nitrophenyloxy) -5-methylpyrazole was reacted with ethanol in the presence of potassium bicarbonate, to give 3- (5-ethoxy-2--2-hydroxypyrazole). A yellow viscous substance (trophenyloxy) -5-methylpyrazole was obtained (yield: 59.8).
  • Example 1 A 3-substituted phenyloxypyrazol derivative having an amino group as in Example 46 (Example 47: 3- (4-aminophenyloxy) -5-methylpyrazole, Example 1 48: 3- (4-amino-3-chlorophenoxy) -5-methylpyrazole, Example 1 49: 3- (4-amino-2-trifluoromethylphenyloxy) -5-methylpyrazole) Was converted to diazonium salt, and the amino group was eliminated to obtain a 3-substituted phenyloxypyrazole derivative.
  • the product / shape / yield / melting point / band R spectrum is described below.
  • Example 1 50 To a mixed solution of concentrated hydrochloric acid (2.1 mL) and acetone (20 mL), add 3- (4-amino-3-trifluoromethylphenyloxy) -5-methylpyrazol (2.00 g, 7.8 bandage 01) at room temperature. Stirred for 20 minutes. After cooling to 0 ° C. or lower, sodium nitrite (0.54 g, 7.8 bandol) dissolved in water (3 mL) was added dropwise, and the mixture was stirred at the same temperature for 30 minutes. Then, cuprous chloride (0.85 g, 8.6 mmol) was added little by little at 0 ° C, and the mixture was stirred for 1 hour at room temperature.
  • Example 1 In the same manner as in Example 50, a diazodium salt was prepared from 3- (4-amino-2-trifluoromethylphenyloxy) -5-methylpyrazole, and reacted with cuprous chloride to prepare a diazodium salt. A pale yellow viscous substance (yield: 56.0%) of-(4-chloro-2-trifluoromethylphenyloxy) -5-methylpyrazole was obtained. Negation RCCDC1 3, TMS, ppm): .
  • Example 1 53 Triethylamine (0.13 g, 1.3 mmol) was added to a solution of 5-methyl-3-phenyloxypyrazol (0.22 g, 1.2 mmol) in ethyl acetate (5 mL), and the mixture was cooled to 0 ° C. Ethyl isocyanate (0.09 g, 1.3 mmol) was added, and the mixture was stirred at the same temperature for 30 minutes and stirred for 4 hours while gradually returning to room temperature. After completion of the reaction, the reaction mixture was poured into 1N hydrochloric acid (10 mL) and extracted with ethyl acetate (10 mL ⁇ 2).
  • Trimethylamine (0.19 g, 1.4 mmol) and phenyl isocyanate were added to a solution of 5-methyl-3--(2_trifluoromethylphenyloxy) pyrazole (0.30 g, 1.2 ol) in ethyl acetate (5 mL).
  • Nate (0.17 g, 1.4 bandol) was added at 0 ° C, and the temperature was gradually returned to room temperature and stirred for 6 hours. After completion of the reaction, the reaction mixture was poured into 1N hydrochloric acid (10 mL) and extracted with ethyl acetate (10 in LX3).
  • the organic layer was washed with water (10 mL ⁇ 2), dried over anhydrous magnesium sulfate, the desiccant was removed by filtration, and the solvent was distilled off from the filtrate under reduced pressure.
  • Example 1 56 5-methyl-3- (3-trifluoromethylphenyloxy) pyrazole and isocyanates
  • Example 1 57 ethyl isocyanate
  • Example 1 5 8 T-butyl isocyanate
  • Example 59 hexyl isocyanate
  • Example 60 cyclohexyl isocyanate
  • Example 1 61 aryl isocyanate
  • Example 1 62 2 -Chloroethyl isocyanate
  • Example 1 63 Ethyl isocyanatoacetate
  • Example 1 65 2-Chlorophenyl phenyl isocyanate
  • Example 16 6 3-chlorophenylisocyanate
  • Example 1 67 3-methylphenylisocyanate
  • Example 1 68 3-nitrophenylisocyanate
  • Example-69 4-methylphenylisocyanate
  • Example 1 70 4-Fluorophenyl isocyanate
  • Example 1 70 4-
  • Triethylamine (0.17 g, 1.65 mmol) was added to a solution of 3- (4-chloro-2--2-trifluoromethylphenyloxy) -5-methylpyrazole (0.55 g, 2.0 mol) in ethyl acetate (5 mL).
  • Ethyl isocyanate (0.31 g, 2.2 mmol) was added, and the mixture was stirred at room temperature for 6 hours. After completion of the reaction, the reaction mixture was poured into 1N hydrochloric acid (10 mL) and extracted with ethyl acetate (10 mL X3).
  • Example 1 85 Triethylamine (0.32 g, 3.2 mmol) and ethyl isocyanate were added to a solution of 3- (4-fluoro-2--2-nitrophenyloxy) -5-methylpyrazole (0.69 g, 2.9 mmol) in ethyl acetate (10 mL). (0.23 g, 3.2 mmol) was added at 0 ° C, and the mixture was gradually returned to room temperature and stirred for 5 hours. After the completion of the reaction, the reaction mixture was poured into 1N-hydrochloric acid (10 mL) and extracted with ethyl acetate (10 mL ⁇ 2).
  • Example 86 5-methyl-3- (2-nitro-4-trifluoromethylphenyloxy) pyrazol and isocyanates (Example 87: methyl isocyanate, Example 88) Ethyl isocyanate, Example 89: propyl isocyanate, Example 90: isopropyl isocyanate) were reacted to obtain corresponding N-substituted lipoxamides.
  • the product / shape / yield / melting point / band R spectrum is described below.
  • Carbonic acid rim (0.61 g, 4.4 mmo 1) was added to a solution of 5-methyl 3- (4-nitro-2-trifluoromethylphenyloxy) pyrazole (1.15 g, 4.0 mmol) in ethyl acetate (10 mL). And propyl isocyanate (0.34 g, 4.0 mmol) were added, and the mixture was stirred at room temperature for 3 hours. After completion of the reaction, the reaction mixture was poured into 2N-hydrochloric acid, and extracted with ethyl acetate (20 mL ⁇ 3).
  • Example 92 5-methyl-3- (4-nitro-2-trifluoromethylphenyloxy) pyrazole and isocyanates (Example 93: methyl iso-
  • Example 93 methyl iso-
  • Example 93 methyl iso-
  • Example 1 94 ethyl isocyanate
  • Example 1 95 isopyl pyrisocyanate
  • Example—N-ethyl-5-methyl-3 was prepared by reacting 5-methyl-3- (3-methoxy-4-nitrophenyloxy) pyrazol with ethyl isocyanate in the same manner as in 96. -(3-Methoxy-4_nitrophenyloxy) pyrazol-1-force A yellow viscous substance of lipoxamide (yield: 62.9) was obtained.
  • N-ethyl was obtained by reacting 3- (5-ethoxy-2-nitrophenyloxy) -5-methylpyrazole and ethyl isocyanate in ethyl acetate in the presence of lithium carbonate in the same manner as in 99.
  • a yellow solid of -3- (5-ethoxy-2-2-toluenephenyloxy) -5-methylpyrazole-1-carboxylamide was obtained (yield: 75.9%).
  • Example 1 1 0 1 Triethylamine (0.17 g, 1.7 mmol) was added to a solution of 3- (4-chloro-3-3-trifluoromethylphenyloxy) -5-methylpyrazole (0.42 g, 1.5 mol) in ethyl acetate (5fflL). Tyl isocyanate (0.12 g, 1.7 mmol) was added at 0 ° C, and the temperature was gradually returned to room temperature and stirred for 5 hours. After completion of the reaction, the reaction mixture was poured into 1N-hydrochloric acid (10 mL) and extracted with ethyl acetate (10 mL ⁇ 2).
  • Example 102 5-methyl-3- (4-nitro-3-trifluoromethylphenyloxy) pyrazole and isocyanates (Example 103: methyl isocyanate, Example 104) : Ethyl isocyanate) in ethyl acetate in the presence of carbon dioxide lysate to obtain the corresponding N-substituted lipoxamides.
  • the product / shape / yield / melting point / NMR spectrum are described below.
  • Triethylamine (0.40 g, 4. Ommol) was added to a solution of 3- (2,6-dichloro-4-trifluoromethylphenyloxy) -5-methylvirazole (1.24 g, 4.0 mmol) in ethyl acetate (20 mL).
  • methyl isocyanate (0.25 g, 4.4 mmol) were added, and the mixture was stirred at room temperature for 6 hours. After completion of the reaction, the reaction mixture was poured into 2N-hydrochloric acid and extracted with ethyl acetate (20 mL ⁇ 3).
  • Example 1 Similar to 105 or 106, 3- (2,6-dichloro-4-trifluoromethylphenyloxy) -5-methylpyrazol and isocyanates (Example 1 107: propyl isocyanate, Example—108: Isopropyl isocyanate, Example 1 109: t-butyl isocyanate, Example 1 110: Hexyl isocyanate, Example 1 111: Octyl isocyanate, Example 1 1 12: aryl isocyanate, Example 1 13: 2-chloroethyl isocyanate, Example—114: 2-bromoethyl isocyanate, Example 1 115: benzyl isocyanate, Example By reacting 116: ethyl isocyanatoacetate, Example-117: 3-ethyl ethyl isocyanatopropionate) in ethyl acetate in the presence of a base, corresponding N-substituted carboxamides were obtained.
  • Example 1-1 3- (2-chloro-6-nitro-4-trifluoromethylphenyloxy) -5-methylpyrazol and isocyanates (Example 1-127: methyl iso- The cyanate, Example-128: propyl isocyanate) were reacted in ethyl acetate in the presence of potassium carbonate to obtain the corresponding N-substituted lipoxamides. Below, product / shape / yield / melting point / awake Enter the R spectrum.
  • Triethylamine (0.22 g, 2.2 mmo I) was added to a solution of 5-methyl-3- (6-methoxy_3_ditropyridine-2-yloxy) pyrazole (0.5 g, 2.0 dishes ol) in ethyl acetate (lOmL), and 0 °
  • ethyl isocyanate (0.16 g, 2.2 marl) was added, and the mixture was stirred at the same temperature for 30 minutes, returned to room temperature, and stirred for 4 hours.
  • the reaction mixture was poured into 1N hydrochloric acid (10 mL) and extracted with ethyl acetate (10 mL ⁇ 2).
  • Example 1 By reacting 5-methyl-3- (4-methyl-5-nitropyridine-2-yloxy) pyrazole with ethyl isocyanate in the presence of triethylamine in the same manner as in 130, There was obtained a yellow viscous substance of 1-ethyl-5-methyl-3_ (4-methyl-5-ditropyridin-2-yloxy) pyrazole-1-caproloxamide (yield: 19.3%).
  • Example 1 1-32- (3-chloro-5-trifluoromethylpyridine-2-yloxy) -5-methylpyrazole and isocyanates (Example 13-3: methyl isocyanate)
  • N-Heptyl-3- (3-chloro-5-trifluoromethylpyridine-2-yloxy) -5-methylpyrazole-1-carboxylamide / colorless viscous substance / yield: 84.9% ⁇ H MR ( CDCl 3 , TMS, ppm): ⁇ 0.75 to 100 (m, 3 ⁇ ), 110 to 1.50 (m, 8H), 1.50 to 1.70 (m, 2H), 2.65 (s, 3H), 3.20 to 3.45 (m, 2H), 6.04 (s, 1H), 6.95 to 7.15 (m, 1H), 8.02 (d, J 2.0Hz, lH), 8.36 (m, 1H).
  • Example 1-153 (3-chloro-5-trifluoromethylpyridine_2-yloxy) -4,5-dimethylpyrazole and isocyanates (Example 1-154: methyl isocyanate)
  • Example 1 155: Ethyl isocyanate) was reacted to obtain the corresponding N-substituted lipoxamide.
  • the product / shape / yield / melting point / band R spectrum is described.
  • Example 1 A 3-substituted phenyloxypyrazole derivative was prepared in the same manner as in Example 166.
  • Example 1 1 67 3- (2,6-Dichroic-4--4-trifluoromethylphenyloxy) -5-isopropylpyrazole,
  • Example 1 168 5-Tributyl-3- (2,6-dichloro) Mouth-4-trifluoromethylphenyloxy) pyrazole,
  • Example 1 169 3- (2,6-Dichro-4--4-trifluoromethylphenyloxy) -4-ethyl-5-methylpyrazole, working Example 1 1 170: 3- (2,6-dichroic-4--4-trifluoromethylphenyloxy) -5-methoxymethylpyrazole,
  • Example 17 1 ⁇ 3- (2,6-dichroic- By reacting 4-trifluoromethylphenyloxy) pyrazol-5-yl ⁇ ethyl acetate) and ethyl iso
  • Triethylamine (0.20 g) was added to a solution of methyl 3- (2,6-dicyclo-4--4-trifluoromethylphenyloxy) pyrazol-5-carboxylate (0.53 g, 1.5 0101) in ethyl acetate (10 mL). , 2. O mmol) and ethyl isocyanate (0.14 g, 2.0 t ol) were added, and the mixture was stirred at room temperature for 6 hours. After completion of the reaction, the reaction mixture was poured into 2N-hydrochloric acid and extracted with ethyl acetate (10 mL ⁇ 3).
  • Example 1 3_ (2,6-Dichloro-4_trifluoromethylphenyioxy) -5-methylpyrazole and isothiocyanates (Example 1-179: methyl isothiocyanate, Example—180: Ethyl isothiocyanate, Example 1 18 1: Propyl isothiocyanate, Example 1 182: Isopropyl isothiocyanate, Example 1 183: Butyl isothiocyanate 184, 2-methoxyethyl isothiocyanate and Example 1 185: tetrahydrofurfuryl isothiocyanate) to give the corresponding N-substituted carpothioamides I got The product / shape / yield / melting point / NMR spectrum are described below.
  • Example 1 1 87 3- (3-chloro-5-trifluoromethylpyridine-2-yloxy) -5-methylpyrazole (1.OOg, 3.6mmol) in DMF (10mL) solution was mixed with carbon dioxide (0.75g, 5.4mmol). ) And methyl isothiocyanate (0.39 g, 5.4 mmol) were added, and the mixture was stirred at room temperature for 8 hours. After completion of the reaction, the reaction mixture was poured into 2N hydrochloric acid and extracted with ethyl acetate (10 mL ⁇ 3). The organic layer was washed with water, dried over anhydrous magnesium sulfate, the desiccant was removed by filtration, and the solvent was distilled off from the filtrate under reduced pressure.
  • Example 1 19 Ethyl isothiocyanate, Example 1 189: Propyl isothiocyanate, Example—190: Isopropyl isothiocyanate, Example 1 19
  • Example 1 butyl isothiocyanate, Example 1 92: aryl isothiocyanate, Example 1 93: 2-methoxymethyl isothiocyanate, Example 1 1
  • Carbonic acid rim (0.76 g, 5.5 mL) was added to a DMF (15 mL) solution of 3- (3-chloromethyl-5-trifluoromethylpyridine-2-yloxy) -5-methylpyrazol (1.39 g, 5.0 t). mmol) and 2-bromoethylisothiocyanate (0.83 g, 5 mmol) were added, and the mixture was stirred at room temperature for 3 hours. After completion of the reaction, the reaction mixture was poured into 2N-hydrochloric acid (30 mL) and extracted with ethyl acetate (30 mL ⁇ 3).
  • Example-By reacting 5-methyl-3- (3-trifluoromethylphenyloxy) pyrazole with trichloromethyl chloroformate and further reacting with tetrahydrofurfurylamine as in 198, -Tetrahydrofurfuryl-5-methyl-3- (3-trifluoromethylphenyloxy) pyrazole-1-potassium lipoxamide as a white solid (yield: 70.3%).
  • Example 1 In the same manner as in Example 201, 3- (2,6-dichloro-4_trifluoromethylphenyloxy) -5-methylpyrazole was reacted with trichloromethyl chloroformate, and then amines ( Example 1 202: s-Butylamine, Example—203: 3-aminopentane, Example 1 204: Cyclopentylamine, Example 1 205: Propargylamine, Example 1 206: 0 -Ethylhydroxylamine hydrochloride, Example-207: 0-t-Butylhydroxylamine, Example 1 208: 0 -Arylhydroxylamine, Example-1209: -0- Benzyl hydroxylamine, Example 1 210: Ethanolamine, Example 1 211: 2,2,2-Trifluoroethylamine, Example 1 212: Tetrahydrofurfurylamine, Example Example 1 2 1 3: Furfurylamine, Example 1 2 1 4: 2-Morpholineethylamine, Example One
  • the product / shape / yield / melting point / band R spectrum is described.
  • Example—Similarly to 223, 3-substituted phenyloxy-5-methylpyrazol (Example—224: 3- (3-chloro-5-trifluoromethylpyridine-2-yloxy) _5-methylpyrazole, Example 1 225: 3- (3-chloro-5-trifluoromethylpyridine-2-yloxy) -5-methylpyrazole, Example 1 226: 5-Methyl-3- (3-trifluoromethylphenyloxy) ) Pyrazole) was reacted with trimethyl chloroformate, and then reacted with aqueous ammonia to obtain the corresponding carboxamide derivatives.
  • the product / shape / yield / melting point / band R spectrum is described below.
  • N-aryl-3- (2,6-dichloro-4-trifluoromethylphenyloxy) -5-methylpyrazol-1-carboxyloxamide (4.3 g, 10.9 marauder.1) was added to ether (50 mL). ) And water (50 mL), add osmium tetroxide (254 mg, 1.00 bandol) in water (60 mL) and sodium periodate (4.7 g, 21.8 mmol), and stir at room temperature. did.
  • Example 1 In the same manner as in 230, N-formylmethyl-3- (2,6-dioctanol-4-trifluoromethylphenyloxy) -5-methylpyrazol-1-hexylpropoxamide and alcohols (implemented Example 1 2 3 1: 1,3-propanediol, Example 2 32: Methanol) were reacted to obtain corresponding lipoxamide derivatives.
  • Example 1 23 1 the product / shape / yield / melting point / ⁇ R spectrum will be described.
  • N-Butyl-3- (3-coguchi-5-trifluoromethylpyridine-2-yloxy) -5-methylpyrazol-1-carbothioamide (0.98 g, 2.5 1)
  • an aqueous hydration solution (0.42 g, 7.5 mmol) and 30% aqueous hydrogen peroxide (2.7 mL)
  • the reaction mixture was extracted with ethyl acetate (15 mL ⁇ 3)
  • the organic layer was washed with water, dried over anhydrous magnesium sulfate, and filtered.
  • Example 1 In the same manner as in Example 23, 3- (3-chloromethyl-5-trifluoromethylpyridine-2-yloxy) -5-1, trifluoromethylpyrazole and a derivative of livamoylc lipide (Example 238: Dimethylcarbamoyl chloride, Example—240-mouth lid, Example 1 24 1: Diisopropyl Luba (Moyl chloride) to give the corresponding lipoxamamide. The product / shape / yield / melting point / band R spectrum is described below.
  • Example 1 238 Dimethylcarbamoyl chloride, Example—240-mouth lid, Example 1 24 1: Diisopropyl Luba (Moyl chloride) to give the corresponding lipoxamamide.
  • the product / shape / yield / melting point / band R spectrum is described below.
  • Example ⁇ , ⁇ -diisopropyl-3- (2-nitro-4-trifluoromethylphenyloxy) -5-trifluoromethylpyrazole-1-potassium lipoxamide was obtained in the same manner as in Example 236. .
  • White solid / Yield:? ⁇ /! ! ⁇ ⁇ ⁇ ! ⁇ ! ! - ⁇ . . 1 3, TMS, ppm): . ⁇ 1.33 (d, J 5.9Hz, 12H), 2.
  • Example 247 The N-methyl form
  • Example 1 248 N-ethyl form
  • N-Ethyl-3_ (3-chloro-5-trifluoromethylpyridine-2-yloxy) -5-methylpyrazole-1-carboxoxamide (0.35 g, 1.0 ol) was dissolved in a solution of sulfuryl chloride (0.3 mL) in acetic acid (5 mL). 0.16 g, 1.2 mniol) and stirred at room temperature for 4 hours. After the completion of the reaction, the reaction mixture was poured into ice water and extracted with ethyl acetate (10 mL ⁇ 3). The organic layer was washed with water, dried over anhydrous magnesium sulfate, the desiccant was removed by filtration, and the solvent was distilled off from the filtrate under reduced pressure.
  • Example 25 Reaction of N-substituted-3- (3-chloromethyl-5-trifluoromethylpyridine-2-yloxy) -5-methylvirazole-1-carboxamide derivative with sulfuryl chloride in the same manner as in 1 By doing so, the corresponding 4-black mouth conductors were obtained.
  • the product / shape / yield / melting point / NMR spectrum is described.
  • N-Methyl-4-chloro-3-3- (3-chloro-5-5-trifluoromethylpyridine_2-yloxy) -5-methylpyrazole-1-hexanoloxamide / white solid / yield: 97.13 ⁇ 4 / ⁇ , 3 ⁇ ), 6.80 to 715 (in, 1H), 8.04 (d, J 2.1Hz, 1H), 8.32 (m, 1H).
  • Me methyl group; Et: ethyl group; Pr: propyl group; i-Pr; isopropyl group; cPr: cyclopropyl group; Bu: butyl group; i-Bu: isobutyl group; T-Bu: tert-butyl group; Pent: pentyl group; C-Pent: cyclopentyl group; Hex: hexyl group; c-Hex: cycle hexyl group; Hep: heptyl group; Oc t: octyl group; Dod: dodecyl group;

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Dentistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Plant Pathology (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

L'invention concerne un dérivé de pyrazole représenté par la formule générale suivante : (1). Ce dérivé est hautement efficace lorsqu'il est utilisé en tant qu'ingrédient actif d'un herbicide.
PCT/JP2002/001411 2001-02-20 2002-02-19 Derives de pyrazole, intermediaires associes, procedes de production associes et herbicide contenant lesdits derives en tant qu'ingredient actif WO2002066439A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US10/468,527 US7700786B2 (en) 2001-02-20 2002-02-19 Pyrazole derivative, intermediate therefor, processes for producing these, and herbicide containing these as active ingredient
AT02712451T ATE504573T1 (de) 2001-02-20 2002-02-19 Pyrazolderivate, deren zwischenprodukte, verfahren zu deren herstellung und herbizid, das diese verbindungen als wirkstoff enthält
DE60239667T DE60239667D1 (de) 2001-02-20 2002-02-19 Pyrazolderivate, deren zwischenprodukte, verfahren zu deren herstellung und herbizid, das diese verbindungen als wirkstoff enthält
JP2002565956A JP4249982B2 (ja) 2001-02-20 2002-02-19 ピラゾール誘導体とその製造中間体及びそれらの製造方法、並びにそれらを有効成分とする除草剤
BR0207412-5A BR0207412A (pt) 2001-02-20 2002-02-19 Derivado de pirazol, seu intermediário, processos para a preparação destes, e herbicida contendo o mesmo como ingrediente ativo
EP02712451A EP1362852B1 (fr) 2001-02-20 2002-02-19 Derives de pyrazole, intermediaires associes, procedes de production associes et herbicide contenant lesdits derives en tant qu'ingredient actif
US12/713,421 US20100152443A1 (en) 2001-02-20 2010-02-26 Pyrazole derivative, intermediate therefor, processes for producing these, and herbicide containing these as active ingredient

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2001-043199 2001-02-20
JP2001043199 2001-02-20

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US12/713,421 Division US20100152443A1 (en) 2001-02-20 2010-02-26 Pyrazole derivative, intermediate therefor, processes for producing these, and herbicide containing these as active ingredient

Publications (1)

Publication Number Publication Date
WO2002066439A1 true WO2002066439A1 (fr) 2002-08-29

Family

ID=18905409

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2002/001411 WO2002066439A1 (fr) 2001-02-20 2002-02-19 Derives de pyrazole, intermediaires associes, procedes de production associes et herbicide contenant lesdits derives en tant qu'ingredient actif

Country Status (8)

Country Link
US (2) US7700786B2 (fr)
EP (2) EP1362852B1 (fr)
JP (1) JP4249982B2 (fr)
AT (1) ATE504573T1 (fr)
BR (1) BR0207412A (fr)
DE (1) DE60239667D1 (fr)
ES (1) ES2363423T3 (fr)
WO (1) WO2002066439A1 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006206473A (ja) * 2005-01-27 2006-08-10 Sagami Chem Res Center ３−ヒドロキシピラゾール−１−カルボキサミド誘導体の製造方法
WO2011043387A1 (fr) 2009-10-08 2011-04-14 エーザイ・アール・アンド・ディー・マネジメント株式会社 Composé de pyrazolooxazole
CN101193864B (zh) * 2005-05-23 2011-12-07 公益财团法人相模中央化学研究所 吡唑-1-甲酸酯衍生物、其制造方法和吡唑衍生物类的制造方法
WO2019016066A1 (fr) 2017-07-18 2019-01-24 Bayer Cropscience Aktiengesellschaft 3-hétéroaryloxy-1h-pyrazoles substitués et leurs sels, et leur utilisation comme agents herbicides

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8097712B2 (en) 2007-11-07 2012-01-17 Beelogics Inc. Compositions for conferring tolerance to viral disease in social insects, and the use thereof
US8962584B2 (en) 2009-10-14 2015-02-24 Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. Compositions for controlling Varroa mites in bees
EA201792402A3 (ru) 2010-03-08 2018-09-28 Монсанто Текнолоджи Ллс Молекулы полинуклеотидов для регуляции генов у растений
WO2013040049A1 (fr) 2011-09-13 2013-03-21 Monsanto Technology Llc Procédés et compositions pour lutter contre les mauvaises herbes
MX348495B (es) 2011-09-13 2017-06-14 Monsanto Technology Llc Metodos y composiciones para el control de malezas.
MX362810B (es) 2011-09-13 2019-02-13 Monsanto Technology Llc Metodos y composiciones para controlar malezas.
US10806146B2 (en) 2011-09-13 2020-10-20 Monsanto Technology Llc Methods and compositions for weed control
US10760086B2 (en) 2011-09-13 2020-09-01 Monsanto Technology Llc Methods and compositions for weed control
UA116089C2 (uk) 2011-09-13 2018-02-12 Монсанто Текнолоджи Ллс Спосіб та композиція для боротьби з бур'янами (варіанти)
WO2013040116A1 (fr) 2011-09-13 2013-03-21 Monsanto Technology Llc Procédés et compositions de lutte contre les mauvaises herbes
US10829828B2 (en) 2011-09-13 2020-11-10 Monsanto Technology Llc Methods and compositions for weed control
WO2013175480A1 (fr) 2012-05-24 2013-11-28 A.B. Seeds Ltd. Compositions et procédés pour le silençage de l'expression génique
US10683505B2 (en) 2013-01-01 2020-06-16 Monsanto Technology Llc Methods of introducing dsRNA to plant seeds for modulating gene expression
CA2896762A1 (fr) 2013-01-01 2014-07-10 A.B. Seeds Ltd. Procedes d'introduction d'arnds dans des graines de plante pour moduler l'expression des genes
MX364458B (es) 2013-03-13 2019-04-26 Monsanto Technology Llc Métodos y composiciones para el control de malezas.
US10612019B2 (en) 2013-03-13 2020-04-07 Monsanto Technology Llc Methods and compositions for weed control
US10568328B2 (en) 2013-03-15 2020-02-25 Monsanto Technology Llc Methods and compositions for weed control
UA122662C2 (uk) 2013-07-19 2020-12-28 Монсанто Текнолоджі Ллс Композиція та спосіб боротьби з leptinotarsa
US9850496B2 (en) 2013-07-19 2017-12-26 Monsanto Technology Llc Compositions and methods for controlling Leptinotarsa
AR098295A1 (es) 2013-11-04 2016-05-26 Monsanto Technology Llc Composiciones y métodos para controlar infestaciones de plagas y parásitos de los artrópodos
UA119253C2 (uk) 2013-12-10 2019-05-27 Біолоджикс, Інк. Спосіб боротьби із вірусом у кліща varroa та у бджіл
US10334848B2 (en) 2014-01-15 2019-07-02 Monsanto Technology Llc Methods and compositions for weed control using EPSPS polynucleotides
WO2015153339A2 (fr) 2014-04-01 2015-10-08 Monsanto Technology Llc Compositions et procédés pour lutter contre les insectes nuisibles
AU2015280252A1 (en) 2014-06-23 2017-01-12 Monsanto Technology Llc Compositions and methods for regulating gene expression via RNA interference
WO2015200539A1 (fr) 2014-06-25 2015-12-30 Monsanto Technology Llc Procédés et compositions pour administrer des acides nucléiques à des cellules végétales et réguler l'expression génique
CN106604993A (zh) 2014-07-29 2017-04-26 孟山都技术公司 用于控制昆虫害虫的组合物和方法
BR112017015705A2 (pt) 2015-01-22 2018-03-20 Monsanto Technology Llc composições e métodos para controle de leptinotarsa
WO2016196738A1 (fr) 2015-06-02 2016-12-08 Monsanto Technology Llc Compositions et procédés pour l'administration d'un polynucléotide dans une plante
WO2016196782A1 (fr) 2015-06-03 2016-12-08 Monsanto Technology Llc Procédés et compositions pour l'introduction d'acides nucléiques dans des plantes
WO2020061412A1 (fr) * 2018-09-20 2020-03-26 Kansas State University Research Foundation Composés présentant une toxicité activée par du cuivre ou du zinc contre une infection microbienne
GB202011068D0 (en) * 2020-07-17 2020-09-02 Syngenta Crop Protection Ag Improvements in or relating to organic compounds

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3923789A (en) * 1973-04-19 1975-12-02 Bayer Ag Penicillins
US3991073A (en) * 1972-02-09 1976-11-09 U.S. Philips Corporation Pyrazoline compounds having insecticidal activity
US4070365A (en) * 1974-07-12 1978-01-24 U.S. Philips Corporation Pyrazoline compounds
JPS559062A (en) * 1978-07-04 1980-01-22 Basf Ag Pyrazole ether derivatives and herbicide containing their compounds
EP0295233A2 (fr) * 1987-06-08 1988-12-14 Monsanto Company 3-(4-Nitrophénoxy)pyrazoles et leur utilisation comme herbicides
EP0370990A1 (fr) * 1988-11-23 1990-05-30 Monsanto Company Pyrazoles substitués à activité herbicide
EP0508469A1 (fr) * 1991-04-11 1992-10-14 Dowelanco 3,4,N-Trisubstitués-4,5-dihydro-1H-pyrazole-1-carboxamides et leur utilisation comme insecticides
US5185025A (en) * 1988-11-21 1993-02-09 Monsanto Company Substituted pyrazoles and their use as herbicides
EP0647612A1 (fr) * 1993-10-07 1995-04-12 American Cyanamid Company Aryloxybenzènes comme agents herbicides
JPH07285962A (ja) * 1994-04-20 1995-10-31 Nissan Chem Ind Ltd ピリジンカルボン酸アミド誘導体
JPH08245594A (ja) * 1995-03-10 1996-09-24 Nissan Chem Ind Ltd ２−オキシアニリン誘導体および除草剤

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2409753A1 (de) * 1974-03-01 1975-09-11 Basf Ag Substituierte pyrazole
US4620865A (en) * 1983-11-07 1986-11-04 Eli Lilly And Company Herbicidal and algicidal 1,5-disubstituted-1H-pyrazole-4-carboxamides
GB8619236D0 (en) 1986-08-06 1986-09-17 Ici Plc Fungicides
US4885022A (en) * 1987-03-17 1989-12-05 Nissan Chemical Industries Ltd. Herbicidal pyrazole derivatives
US4964895A (en) * 1987-06-08 1990-10-23 Monsanto Company Substituted 4-(4-nitrophenoxy) pyrazoles and their use as herbicides
US4948902A (en) * 1988-04-13 1990-08-14 Monsanto Company Process for making substituted pyrazoles
KR930004672B1 (ko) * 1988-08-31 1993-06-03 니혼 노야꾸 가부시끼가이샤 3-치환 페닐피라졸 유도체 또는 이의 염 및 이의 제조방법, 이의 용도 및 이의 사용 방법
ATE159938T1 (de) 1990-12-17 1997-11-15 Sankyo Co Pyrazolderivate mit herbizider wirkung, deren herstellung und verwendung
DE19542520A1 (de) * 1995-11-15 1997-05-22 Basf Ag Substituierte 1-Methyl-3-phenylpyrazole
DE19548786A1 (de) 1995-12-27 1997-07-03 Basf Ag 2-Pyrazolyloxy- und 2-Triazolyloxyphenylessigsäure-Derivate, sie enthaltende Mittel und ihre Verwendung zur Bekämpfung von Schadpilzen und tierischen Schädlingen
US7767828B2 (en) * 2003-11-12 2010-08-03 Phenomix Corporation Methyl and ethyl substituted pyrrolidine compounds and methods for selective inhibition of dipeptidyl peptidase-IV

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3991073A (en) * 1972-02-09 1976-11-09 U.S. Philips Corporation Pyrazoline compounds having insecticidal activity
US3923789A (en) * 1973-04-19 1975-12-02 Bayer Ag Penicillins
US4070365A (en) * 1974-07-12 1978-01-24 U.S. Philips Corporation Pyrazoline compounds
JPS559062A (en) * 1978-07-04 1980-01-22 Basf Ag Pyrazole ether derivatives and herbicide containing their compounds
EP0295233A2 (fr) * 1987-06-08 1988-12-14 Monsanto Company 3-(4-Nitrophénoxy)pyrazoles et leur utilisation comme herbicides
US5185025A (en) * 1988-11-21 1993-02-09 Monsanto Company Substituted pyrazoles and their use as herbicides
EP0370990A1 (fr) * 1988-11-23 1990-05-30 Monsanto Company Pyrazoles substitués à activité herbicide
EP0508469A1 (fr) * 1991-04-11 1992-10-14 Dowelanco 3,4,N-Trisubstitués-4,5-dihydro-1H-pyrazole-1-carboxamides et leur utilisation comme insecticides
EP0647612A1 (fr) * 1993-10-07 1995-04-12 American Cyanamid Company Aryloxybenzènes comme agents herbicides
JPH07285962A (ja) * 1994-04-20 1995-10-31 Nissan Chem Ind Ltd ピリジンカルボン酸アミド誘導体
JPH08245594A (ja) * 1995-03-10 1996-09-24 Nissan Chem Ind Ltd ２−オキシアニリン誘導体および除草剤

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
ABUZAR S. ET AL.: "A new convenient method of desulphurisation of thioureas & thiomamides", INDIAN J. CHEM., SECT. B, vol. 19B, 1980, pages 211 - 212, XP002952603 *
ALLAH H.M. ET AL.: "Potential antineoplastic agents", PHARMAZIE, vol. 35, no. 12, 1980, pages 799 - 800, XP002952602 *
CLARK R.D.: "Synthesis and QSAR of herbicidal 3-pyrazolyl alpha,alpha,alpha-trifluorotolyl ethers", J. AGRIC. FOOD CHEM., vol. 44, 1996, pages 3643 - 3652, XP002951900 *
FRECHE P. ET AL.: "Contribution a l'etude de la transformation thermique des aldazines alpha-ethyleneniques. Nouvelle voie d'acces aux pyrazoles halogenes ou substitutes par des groupments phenoxy, thiophenoxy et thioethoxy en 3(5)", TETRAHEDRON, vol. 33, 1977, pages 2069 - 2077, XP002951899 *
NANDIHALLI U.B. ET AL.: "Enantioselectivity of proto-phyrinogen oxidase-inhibiting herbicides", PESTIC. SCI., vol. 40, 1994, pages 265 - 277, XP002952601 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006206473A (ja) * 2005-01-27 2006-08-10 Sagami Chem Res Center ３−ヒドロキシピラゾール−１−カルボキサミド誘導体の製造方法
JP4690733B2 (ja) * 2005-01-27 2011-06-01 公益財団法人相模中央化学研究所 ３−ヒドロキシピラゾール−１−カルボキサミド誘導体の製造方法
CN101193864B (zh) * 2005-05-23 2011-12-07 公益财团法人相模中央化学研究所 吡唑-1-甲酸酯衍生物、其制造方法和吡唑衍生物类的制造方法
WO2011043387A1 (fr) 2009-10-08 2011-04-14 エーザイ・アール・アンド・ディー・マネジメント株式会社 Composé de pyrazolooxazole
WO2019016066A1 (fr) 2017-07-18 2019-01-24 Bayer Cropscience Aktiengesellschaft 3-hétéroaryloxy-1h-pyrazoles substitués et leurs sels, et leur utilisation comme agents herbicides

Also Published As

Publication number Publication date
US20050070441A1 (en) 2005-03-31
BR0207412A (pt) 2004-02-25
US20100152443A1 (en) 2010-06-17
EP2292606A1 (fr) 2011-03-09
JP4249982B2 (ja) 2009-04-08
ES2363423T3 (es) 2011-08-03
EP1362852B1 (fr) 2011-04-06
DE60239667D1 (de) 2011-05-19
EP1362852A1 (fr) 2003-11-19
ATE504573T1 (de) 2011-04-15
JPWO2002066439A1 (ja) 2004-06-17
US7700786B2 (en) 2010-04-20
EP1362852A4 (fr) 2004-03-03

Similar Documents

Publication Publication Date Title
WO2002066439A1 (fr) Derives de pyrazole, intermediaires associes, procedes de production associes et herbicide contenant lesdits derives en tant qu&#39;ingredient actif
EP1464642B1 (fr) Nouveau derive de pyrazole substitue, procede de production de ce derive et composition herbicide le contenant
US6107251A (en) Oxazole derivative, process for producing the same, and herbicide
FR2812633A1 (fr) Derives de phenyl(thio)urees et phenyl(thio)carbamates fongicides
EP3619201B1 (fr) 4-difluoro-méthyl benzoylamide à efficacité herbicide
JPH07501549A (ja) ピラゾールカルボキサニリド殺菌剤
SK35993A3 (en) Herbicidal substituted aryl-haloalkylpyrazoles
JP2002145707A (ja) Ｎ−置換ジヒドロピロール誘導体を含有する除草剤
US9988347B2 (en) Herbicidally active arylcarboxylic acid amides
HUT72171A (en) 1-aryltriazolin(thi)ones and process for production of herbicide compositions
EP2595963B1 (fr) 4-(4-halogénoalkyle-3-thiobenzoyle)-pyrazoles et leur utilisation comme herbicides
HU196030B (en) Herbicides comprising substituted 5-(acylamino)-1-phenyl-pyrazole derivatives and active ingredient and process for producing substituted 5-(acylamino)-1-phenyl-pyrazole derivatives
WO2001023358A1 (fr) Derives pyrazole, intermediaires pour la preparation de ces derives, procedes de preparation des derives et intermediaires, et herbicides dont ces derives sont le principe actif
PL115642B1 (en) Pesticide
Ohno et al. Synthesis and herbicidal activity of new pyrazole-4-carboxamide derivatives
DE3903799A1 (de) N-aryl-stickstoffheterocyclen
EP1219173B1 (fr) Insecticides et acaricides
SK159697A3 (en) Herbicidal substituted 3-aryl-pyrazoles
WO1999052881A1 (fr) Derives de 2-anilinopyrimidinone, intermediaires utilises dans la production de ceux-ci, procede de production correspondant et pesticides contenant ces derives comme principe actif
JPH02193976A (ja) ３―フェノキシピラゾール誘導体、その製造法およびその使用
WO2000029387A1 (fr) Derives de 2- anilino (3h)- pyrimidone, intermediaires dans la production de ces derniers, procede de production de ces derniers et pesticides contenant ces derniers comme ingredient actif
JPH01230562A (ja) フェニルトリアゾール誘導体及び殺虫剤
TWI229662B (en) Novel benzamidoxime derivatives and intermediates, their preparation and their use as fungicides
JPH06100550A (ja) ジアゾール誘導体および有害生物防除剤
JPS61286380A (ja) １−アリ−ル−４−ヘテロサイクリル−ピラゾ−ル類

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2002565956

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 2002712451

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 2002712451

Country of ref document: EP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWE Wipo information: entry into national phase

Ref document number: 10468527

Country of ref document: US